Neddylation inhibitor MLN4924 suppresses growth and migration of human gastric cancer cells

被引:79
|
作者
Lan, Huiyin [1 ,2 ]
Tang, Zaiming [1 ]
Jin, Hongchuan [2 ]
Sun, Yi [1 ,3 ,4 ]
机构
[1] Zhejiang Univ, Inst Translat Med, Sch Med, Hangzhou 310029, Zhejiang, Peoples R China
[2] Zhejiang Univ, Inst Clin Sci, Sir Run Run Shaw Hosp, Lab Canc Biol,Sch Med, Hangzhou 310020, Zhejiang, Peoples R China
[3] Zhejiang Univ, Collaborat Innovat Ctr Diag & Treatment Infect Di, Hangzhou 310003, Zhejiang, Peoples R China
[4] Univ Michigan, Div Radiat & Canc Biol, Dept Radiat Oncol, 4424B MS-1,1301 Catherine St, Ann Arbor, MI 48109 USA
来源
SCIENTIFIC REPORTS | 2016年 / 6卷
基金
中国国家自然科学基金;
关键词
NEDD8-ACTIVATING ENZYME-INHIBITOR; E3 UBIQUITIN LIGASE; CULLIN-RING LIGASES; G(2)/M CHECKPOINT; S-PHASE; APOPTOSIS; ANTICANCER; ACTIVATION; SENESCENCE; INDUCTION;
D O I
10.1038/srep24218
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
MLN4924 is a recently discovered small molecule inhibitor of NEDD8-Activating Enzyme (NAE). Because cullin RING ligase (CRL), the largest family of E3 ubiquitin ligase, requires cullin neddylation for its activity, MLN4924, therefore, acts as an indirect inhibitor of CRL by blocking cullin neddylation. Given that CRLs components are up-regulated, whereas neddylation modification is over-activated in a number of human cancers, MLN4924 was found to be effective in growth suppression of cancer cells. Whether MLN4924 is effective against gastric cancer cells, however, remains elusive. Here we showed that in gastric cancer cells, MLN4924 rapidly inhibited cullin 1 neddylation and remarkably suppressed growth and survival as well as migration in a dose-and time-dependent manner. Mechanistic studies in combination with siRNA knockdown-based rescue experiments revealed that MLN4924 induced the accumulation of a number of CRL substrates, including CDT1/ORC1, p21/p27, and PHLPP1 to trigger DNA damage response and induce growth arrest at the G2/M phase, to induce senescence, as well as autophagy, respectively. MLN4924 also significantly suppressed migration by transcriptionally activating E-cadherin and repressing MMP-9. Taken together, our study suggest that neddylation modification and CRL E3 ligase are attractive gastric cancer targets, and MLN4924 might be further developed as a potent therapeutic agent for the treatment of gastric cancer.
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收藏
页数:12
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